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  4. ISO 19001:2013

ISO 19001:2013

In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology

General Information

Status : Active

Standard Type : Main

Document No :
ISO 19001:2013

Document Year : 2013

Pages : 14

Edition : 2

Section Volume : Clinical laboratory testing and in vitro diagnostic test systems (ISO/TC 212.)

ICS : Diagnostic equipment (11.040.55)In vitro diagnostic test systems (11.100.10)
ISO 19001:2013 specifies requirements for information supplied by the manufacturer with reagents used in staining in biology. It applies to producers, suppliers and vendors of dyes, stains, chromogenic reagents and other reagents used for staining in histology and cytology including bacteriology, haematology, histochemistry, as performed in medical laboratories, both routine and research bacteriology. The requirements for information supplied by the manufacturer specified in ISO 19001:2013 are a prerequisite for achieving comparable and reproducible results in all fields of staining in biology.

Life Cycle

WITHDRAWN
ISO 19001:2002
ACTIVE
ISO 19001:2013
WITHDRAWN
ISO 19001:2002
ACTIVE
ISO 19001:2013
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Format available